(2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane

Base Information

Chemical Name:(2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane
CAS No.:142128-66-3
Molecular Formula:C₂₃H₂₅BrCl₂N₂O₄
Molecular Weight:544.273
Hs Code.:

Synonyms:(2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane

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Technology Process of (2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane

There total 3 articles about (2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 2631-72-3
2,4-dichlorophenacyl bromide

: 142128-66-3
(2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane

Guidance literature:: Multi-step reaction with 2 steps

1: 34 percent / p-TsOH, n-BuOH / toluene / 5 h / Heating

2: 1.) NaH / 1.) DMSO, RT, 1 h, 2.) DMSO, 80 deg C, 5 h

With sodium hydride; toluene-4-sulfonic acid; butan-1-ol; In toluene;
DOI:10.1021/jm00093a015

Reference yield:

: 2234-16-4
1-(2,4-dichlorophenyl)ethan-1-one

: 142128-66-3
(2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / copper(II) bromide / ethyl acetate; CH₂Cl₂ / 16 h / Heating

2: 34 percent / p-TsOH, n-BuOH / toluene / 5 h / Heating

3: 1.) NaH / 1.) DMSO, RT, 1 h, 2.) DMSO, 80 deg C, 5 h

With sodium hydride; toluene-4-sulfonic acid; copper(ll) bromide; butan-1-ol; In dichloromethane; ethyl acetate; toluene;
DOI:10.1021/jm00093a015

Reference yield:

: 82966-35-6,113770-66-4,142128-61-8,142128-62-9,142128-63-0,142128-64-1
(2R,4S)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<<(4-methylphenyl)sulfonyl>oxy>methyl>-1,3-dioxolane

: 67914-60-7,89929-31-7
N-acetyl-N'-(4-hydroxyphenyl)piperazine

: 142128-66-3
(2R,4R)-trans-2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-<<4-(4-acetylpiperazin-1-yl)phenoxy>methyl>-1,3-dioxolane

Guidance literature:: With sodium hydride; Yield given. Multistep reaction; 1.) DMSO, RT, 1 h, 2.) DMSO, 80 deg C, 5 h;
DOI:10.1021/jm00093a015